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International Journal of Legal Medicine
|
June 21, 2012
Forensic performance of two insertion-deletion marker assays
M Fondevila, C Phillips, C Santos, et al.
Forensic Science International
|
February 1, 1992
A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques
P Gill, S Woodroffe, W Bär, et al.
Research Square
|
June 12, 2026
Non-coding Regulatory Variants in ASD (Autism Spectrum Disorders) Disrupt CTCF Domains and Shape Cell-Type-Specific Neurodevelopmental Landscapes Revealed by Single-Cell Analyses and Cortical Organoids
Sara Dominguez-Alonso, P Carballo-Pacoret, Jr Paul Trotta, et al.
Forensic Science International. Genetics
|
December 17, 2008
DNA Commission of the International Society for Forensic Genetics (ISFG): recommendations regarding the role of forensic genetics for disaster victim identification (DVI)
M Prinz, A Carracedo, W R Mayr, et al.
Forensic Science International. Genetics
|
December 17, 2008
D9S1120, a simple STR with a common Native American-specific allele: forensic optimization, locus characterization and allele frequency studies
C Phillips, A Rodriguez, A Mosquera-Miguel, et al.
Forensic Science International. Genetics
|
September 13, 2011
A new SNP assay for identification of highly degraded human DNA
A Freire-Aradas, M Fondevila, A-K Kriegel, et al.
Parasitology
|
November 19, 2013
High-throughput genotyping assay for the large-scale genetic characterization of Cryptosporidium parasites from human and bovine samples
J L Abal-Fabeiro, X Maside, J Llovo, et al.
International Journal of Legal Medicine
|
May 17, 2014
Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications
M Alcalde, O Campuzano, C Allegue, et al.
The British Journal of Ophthalmology
|
September 26, 2008
Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa
A J Brea-Fernández, E Pomares, M J Brión, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
May 2, 2008
[18F-fluoro-L-DOPA PET-CT imaging combined with genetic analysis for optimal classification and treatment in a child with severe congenital hyperinsulinism]
J Arbizu Lostao, A Fernández-Marmiesse, P Garrastachu Zumarrán, et al.
Page
of 23
Search research articles
Search
Showing results (151-160 of 223) with videos related to
Sort By:
Page
of 23
International Journal of Legal Medicine
|
June 21, 2012
Forensic performance of two insertion-deletion marker assays
M Fondevila, C Phillips, C Santos, et al.
Forensic Science International
|
February 1, 1992
A report of an international collaborative experiment to demonstrate the uniformity obtainable using DNA profiling techniques
P Gill, S Woodroffe, W Bär, et al.
Research Square
|
June 12, 2026
Non-coding Regulatory Variants in ASD (Autism Spectrum Disorders) Disrupt CTCF Domains and Shape Cell-Type-Specific Neurodevelopmental Landscapes Revealed by Single-Cell Analyses and Cortical Organoids
Sara Dominguez-Alonso, P Carballo-Pacoret, Jr Paul Trotta, et al.
Forensic Science International. Genetics
|
December 17, 2008
DNA Commission of the International Society for Forensic Genetics (ISFG): recommendations regarding the role of forensic genetics for disaster victim identification (DVI)
M Prinz, A Carracedo, W R Mayr, et al.
Forensic Science International. Genetics
|
December 17, 2008
D9S1120, a simple STR with a common Native American-specific allele: forensic optimization, locus characterization and allele frequency studies
C Phillips, A Rodriguez, A Mosquera-Miguel, et al.
Forensic Science International. Genetics
|
September 13, 2011
A new SNP assay for identification of highly degraded human DNA
A Freire-Aradas, M Fondevila, A-K Kriegel, et al.
Parasitology
|
November 19, 2013
High-throughput genotyping assay for the large-scale genetic characterization of Cryptosporidium parasites from human and bovine samples
J L Abal-Fabeiro, X Maside, J Llovo, et al.
International Journal of Legal Medicine
|
May 17, 2014
Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications
M Alcalde, O Campuzano, C Allegue, et al.
The British Journal of Ophthalmology
|
September 26, 2008
Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa
A J Brea-Fernández, E Pomares, M J Brión, et al.
Anales De Pediatria (Barcelona, Spain : 2003)
|
May 2, 2008
[18F-fluoro-L-DOPA PET-CT imaging combined with genetic analysis for optimal classification and treatment in a child with severe congenital hyperinsulinism]
J Arbizu Lostao, A Fernández-Marmiesse, P Garrastachu Zumarrán, et al.
Page
of 23